1qh加的频率和遗传效应。 - Suppr

Suppr

超能文献

Frequency and genetic effect of 1qh plus.

作者信息

Nielsen J, Friedrich U, Hreidarsson A B

出版信息

Humangenetik. 1974 Feb 21;21(2):193-6. doi: 10.1007/BF00281037.

DOI:10.1007/BF00281037

PMID:4134842

Abstract

摘要

相似文献

Frequency and genetic effect of 1qh plus.1qh加的频率和遗传效应。

Humangenetik. 1974 Feb 21;21(2):193-6. doi: 10.1007/BF00281037.

Autosomal reciprocal translocations in newborn children and their relatives.新生儿及其亲属中的常染色体相互易位

Humangenetik. 1974 Feb 21;21(2):133-44. doi: 10.1007/BF00281032.

Induction of distinctive chromosomal bands in selected human subjects with D, G, and Y chromosome anomalies.在选定的患有D、G和Y染色体异常的人类受试者中诱导出独特的染色体带。

Hum Hered. 1973 Apr;23(4):313-30. doi: 10.1159/000152592.

Frequency of deletion of short arm satellites in acrocentric chromosomes.近端着丝粒染色体短臂卫星序列缺失的频率

J Med Genet. 1974 Jun;11(2):177-80. doi: 10.1136/jmg.11.2.177.

Are 1q plus chromosomes harmless?1q 加染色体无害吗？

Clin Genet. 1974;6(5):383-93.

Chromosome studies in 5,049 consecutive newborn children.对5049名连续出生的新生儿进行染色体研究。

Clin Genet. 1973;4(4):333-43. doi: 10.1111/j.1399-0004.1973.tb01928.x.

Giemsa banding of chromosome 1gh+ and linkage analysis.1号染色体长臂Giemsa显带及连锁分析。

J Med Genet. 1975 Mar;12(1):44-8. doi: 10.1136/jmg.12.1.44.

Microdensitometric identification of the pericentric inversion of chromosome No.2 and of duplication of the short arm of chromosome No.7 in a reexamined case.在一例复查病例中，通过微密度测定法鉴定2号染色体的臂间倒位和7号染色体短臂的重复。

Hum Hered. 1973 Apr;23(4):331-7. doi: 10.1159/000152593.

Prevalence of chromosome abnormalities among males examined for military service.应征入伍男性中染色体异常的患病率。

Clin Genet. 1973;4(5):422-8. doi: 10.1111/j.1399-0004.1973.tb01171.x.

Inherited pericentric inversion of chromosome number two: a linkage study.2号染色体遗传性臂间倒位：一项连锁研究。

Ann Hum Genet. 1969 Jul;33(1):53-9. doi: 10.1111/j.1469-1809.1969.tb01629.x.

引用本文的文献

Pericentric inversions. Problems and significance for clinical genetics.臂间倒位。临床遗传学中的问题及意义。

Hum Genet. 1984;68(1):1-47. doi: 10.1007/BF00293869.

本文引用的文献

Partial-trisomy syndromes. II. An insertion as cause of the OFD syndrome in mother and daughter.部分三体综合征。II. 一次插入作为母亲和女儿患口面指综合征的病因

Chromosoma. 1961;12:573-84. doi: 10.1007/BF00328943.

A FAMILIAL CHROMOSOME VARIANT IN A SUBJECT WITH ANOMALOUS SEX DIFFERENTIATION.一名性分化异常患者的家族性染色体变异

Am J Hum Genet. 1963 Dec;15(4):465-75.

Chromosomal study in patients with cysts of the jaw, multiple nevoid basal cell carcinomata and bifid rib syndrome.颌骨囊肿、多发性痣样基底细胞癌和肋骨分叉综合征患者的染色体研究

Chromosoma. 1963;14:146-53. doi: 10.1007/BF00336756.

[Asynchronous reduplication in length difference between homologous chromosomes A-1 in man].

Exp Cell Res. 1967 Apr;46(1):58-64. doi: 10.1016/0014-4827(67)90408-9.

[Apert's syndrome (acrocephalo-syndactyly). A case with 1 abnormal chromosome].

Arch Fr Pediatr. 1966 Oct;23(8):887-97.

[Cytogenetic study of a mother and her son presenting the same ocular malformation].

Bull Soc Belge Ophtalmol. 1964;138:602-11.

Asymmetry of chromosome number 1 pair in three generations of a phenotypically normal family.

Can J Genet Cytol. 1968 Sep;10(3):575-89. doi: 10.1139/g68-076.

Chronology and pattern of human chromosome replication. VI. Further studies including autoradiographic behavior of normal and abnormal no. 1 autosomes.人类染色体复制的时间顺序和模式。VI. 进一步的研究，包括正常和异常1号常染色体的放射自显影行为。

Cytogenetics. 1967;6(5):357-70.

[Elongated, submetacentric chromosome no. 1. A very rare heterozygote variant in man].

Humangenetik. 1970 Aug 17;10(1):58-67. doi: 10.1007/BF00297641.

Probable assignment of the Duffy blood group locus to chromosome 1 in man.人类达菲血型位点可能定位于1号染色体。

Proc Natl Acad Sci U S A. 1968 Nov;61(3):949-55. doi: 10.1073/pnas.61.3.949.

文献检索

告别复杂PubMed语法，用中文像聊天一样搜索，搜遍4000万医学文献。AI智能推荐，让科研检索更轻松。

立即免费搜索

文件翻译

保留排版，准确专业，支持PDF/Word/PPT等文件格式，支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述，25分钟生成高质量综述，智能提取关键信息，辅助科研写作。

立即免费体验